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Gershoni-Baruch syndrome: First report of a surviving child

  • Published:2015-12-06 Issue:3 Volume:170 Page:707-711
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Valfrè Laura1,Baban Anwar2,Digilio Maria Cristina3,Bevilacqua Francesca1,Bagolan Pietro1,Conforti Andrea1

Affiliation:

1. Department of Medical and Surgical Neonatology; Bambino Gesù Children Hospital; Rome Italy

2. Department of Cardiology and Cardiosurgery; Bambino Gesù Children Hospital; Rome Italy

3. Department of Medical Genetics; Bambino Gesù Children Hospital; Rome Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference5 articles.

1. Recurrence of diaphragmatic agenesis associated with multiple midline defects: Evidence for an autosomal gene regulating the midline;Bird;Am J Med Genet,1994

2. Heterogeneity in omphalocele with absent radial ray complex;Devriendt;Am J Med Genet,1999

3. Gershoni-Baruch syndrome: Report of a new family confirming autosomal recessive inheritance;Franceschini;Am J Med Genet Part A,2003

4. Unknown syndrome: Radial ray defects, omphalocele, diaphragmatic hernia and hepatic cyst;Gershoni-Baruch;J Med Genet,1990

5. Omphalocele, radial ray defect and diaphragmatic hernia: Another case of Gershoni-Baruch syndrome;Oudesluijs;Genet Couns,2014

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A gershoni-baruch syndrome variant or a new association;Journal of Clinical Neonatology;2021
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